drugset / Trial / NCT00928668
Efficacy (Bronchoprotection) and Safety of Orally Inhaled BI 1744 CL in Patients With Intermittent Asthma
RandomizedCrossoverDouble-blindTreatment
Summary
The primary objective of this study is to assess the efficacy (bronchoprotection) and safety of single doses of BI 1744 CL inhalation solution (2, 5, 10 and 20 mcg) delivered via the Respimat® inhaler, in patients with intermittent asthma.
Timeline
- Start
- 2006-01
- Primary completion
- 2006-10
- Completion
- —
Outcome
Met primary endpoint
registry Placebo vs Olodaterol (Olo) 2 mcg qd; p <0.0001; Mean Difference (Final Values) 1.157 (95% CI 0.657 to 1.657); Mixed Models Analysis NCT00928668 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Olodaterol | Small molecule | 2 ug | Inhaled |
| Subject | Olodaterol | Small molecule | 5 ug | Inhaled |
| Subject | Olodaterol | Small molecule | 10 ug | Inhaled |
| Subject | Olodaterol | Small molecule | 20 ug | Inhaled |